Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling. - Wikidata - awgldk - TriplyDB

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

http://www.wikidata.org/entity/Q38497253

about

Potential biotechnological capabilities of cultivable mycobiota from carwash effluents.Synthesis and properties of fluorescent 4'-azulenyl-functionalized 2,2':6',2″-terpyridines Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.Azulene-boronate esters: colorimetric indicators for fluoride in drinking water.Aromatic metamorphosis: conversion of an aromatic skeleton into a different ring system.Synthesis of 2-Aminofurans by Sequential [2+2] Cycloaddition-Nucleophilic Addition of 2-Propyn-1-ols with Tetracyanoethylene and Amine-Induced Transformation into 6-Aminopentafulvenes.Azulene-Based Donor-Acceptor Systems: Synthesis, Optical, and Electrochemical Properties.Metal-free C-H thioarylation of arenes using sulfoxides: a direct, general diaryl sulfide synthesis.Palladium-Catalyzed Arylation of Arylboronic Acids with Yagupolskii-Umemoto Reagents.One-pot borylation/Suzuki-Miyaura sp2-sp3 cross-coupling.Dual vicinal functionalisation of heterocycles via an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade.

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P2860

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

http://www.wikidata.org/entity/Q38497253

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

@en

type

label

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

@en

prefLabel

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

@en

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P1433

Angewandte Chemie International Edition

P1476

Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

@en

P2093

Gabriele Kociok-Köhn

http://www.w3.org/2001/XMLSchema#string

Michael D Turton

http://www.w3.org/2001/XMLSchema#string

Yu Jin

http://www.w3.org/2001/XMLSchema#string

P2860

Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions

Synthesis of beta-(1-azulenyl)-L-alanine as a potential blue-colored fluorescent tryptophan analog and its use in peptide synthesis

A ring expansion-annulation strategy for the synthesis of substituted azulenes. Preparation and Suzuki coupling reactions of 1-azulenyl triflates.

A review of HNS-32: a novel azulene-1-carboxamidine derivative with multiple cardiovascular protective actions.

Painting proteins blue: β-(1-azulenyl)-L-alanine as a probe for studying protein-protein interactions.

Novel azulene-based derivatives as potent multi-receptor tyrosine kinase inhibitors.

Developing a peptide-based near-infrared molecular probe for protease sensing.

β-(1-Azulenyl)-L-alanine--a functional probe for determination of pKa of histidine residues.

Azulene based metal-organic frameworks for strong adsorption of H2.

An azulene dimer as a near-infrared quencher.

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2564-2568

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scholarly article

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10.1002/ANIE.201510666

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7

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55

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26806850

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4755203

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